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Which metals are dissolved by acetic acid and why it matters

Acetic acid attacks most reactive metals, turning them into soluble acetates and releasing hydrogen, while noble metals stay intact and stainless steel survives only under limited conditions.

Reactive metals that dissolve

Metals that sit high on the electrochemical series lose electrons to the hydrogen ions in acetic acid. The general reaction is:

  • Zn + 2 CH₃COOH → Zn(CH₃COO)₂ + H₂↑
  • Mg + 2 CH₃COOH → Mg(CH₃COO)₂ + H₂↑
  • Al + 3 CH₃COOH → Al(CH₃COO)₃ + 3⁄2 H₂↑
  • Fe (carbon steel) + 2 CH₃COOH → Fe(CH₃COO)₂ + H₂↑

Zinc and magnesium react very quickly, even in dilute solutions. Aluminum’s protective oxide layer dissolves slowly, especially above 60 °C, exposing the metal underneath. Carbon steel corroces at a noticeable rate in 5–10 % acetic acid, producing ferrous acetate.

Metals that resist

Gold, platinum and other noble metals have such low reactivity that acetic acid cannot displace hydrogen from them; no visible reaction occurs.

Copper is a borderline case. In deaerated, dilute acid it shows little change, but when oxygen is present the surface oxidises and a green copper acetate crust forms over weeks.

Stainless steel – conditional resistance

Grade 316 stainless steel, with 2–3 % molybdenum, tolerates dilute, room‑temperature acetic acid because its chromium‑oxide film remains intact. At temperatures above 80 °C or in concentrations above 20 %, the film can be breached, leading to pitting. Grade 304 lacks sufficient molybdenum and pits more readily under the same conditions.

How concentration, water and temperature influence corrosion

Pure glacial acetic acid (≈99.8 %) is less aggressive than a 10 % aqueous solution at room temperature because it contains little water to ionise into H⁺ and CH₃COO⁻. However, acetic acid is hygroscopic; even a small amount of absorbed moisture creates a conductive medium and dramatically speeds up attack.

Temperature follows the usual rule of thumb: a 10 °C rise roughly doubles the reaction rate. Heating a 5 % solution to 100 °C can change a slow surface etch into measurable material loss within hours.

Role of dissolved oxygen

Oxygen acts as a depolariser for metals such as copper and certain alloys. Removing oxygen with deaeration columns can suppress corrosion to near‑zero rates, allowing cheaper materials to be used in closed‑loop systems.

Practical guidelines

  • Use zinc‑ or magnesium‑free alloys when handling concentrated acetic acid.
  • Prefer 316 stainless or higher‑grade alloys for hot, concentrated streams.
  • Keep water content low and control temperature to limit attack on vulnerable metals.
  • Consider deaeration if copper or nickel alloys are required.

❓ Frequently Asked Questions

1. Can vinegar (5 % acetic acid) corrode household metal fixtures?

Yes, it will slowly eat away at zinc‑galvanised bolts and unprotected steel, but the effect is usually visible only after weeks of continuous exposure.

2. Is stainless steel 304 safe for storing glacial acetic acid?

Not at elevated temperatures; 304 can pit in hot, concentrated acid, so 316 or a higher‑grade alloy is recommended for such conditions.

3. Why does copper develop a green layer in vinegar?

Atmospheric oxygen dissolves in the acid, allowing copper to oxidise and form copper acetate, which appears as a blue‑green patina.

4. Does adding water to glacial acetic acid increase corrosion?

Yes, a small amount of water enables ionisation, creating H⁺ and acetate ions that accelerate metal dissolution.